1-Oxo-2,3-dihydro-1H-pyrrolizine-7-carbaldehyde

Details

Top
Internal ID 3cdd1455-8819-4f6b-8670-61f2942f4b35
Taxonomy Organoheterocyclic compounds > Pyrrolizines
IUPAC Name 7-oxo-5,6-dihydropyrrolizine-1-carbaldehyde
SMILES (Canonical) C1CN2C=CC(=C2C1=O)C=O
SMILES (Isomeric) C1CN2C=CC(=C2C1=O)C=O
InChI InChI=1S/C8H7NO2/c10-5-6-1-3-9-4-2-7(11)8(6)9/h1,3,5H,2,4H2
InChI Key PMACSXXWMPSEIU-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C8H7NO2
Molecular Weight 149.15 g/mol
Exact Mass 149.047678466 g/mol
Topological Polar Surface Area (TPSA) 39.10 Ų
XlogP -0.10
Atomic LogP (AlogP) 0.89
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

Top
27792-84-3
1-Oxo-2,3-dihydro-1H-pyrrolizine-7-carbaldehyde

2D Structure

Top
2D Structure of 1-Oxo-2,3-dihydro-1H-pyrrolizine-7-carbaldehyde

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9959 99.59%
Caco-2 + 0.8838 88.38%
Blood Brain Barrier + 0.9379 93.79%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.7370 73.70%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9157 91.57%
OATP1B3 inhibitior + 0.9522 95.22%
MATE1 inhibitior - 0.6800 68.00%
OCT2 inhibitior - 0.5914 59.14%
BSEP inhibitior - 0.9513 95.13%
P-glycoprotein inhibitior - 0.9804 98.04%
P-glycoprotein substrate - 0.9606 96.06%
CYP3A4 substrate - 0.6598 65.98%
CYP2C9 substrate - 0.5798 57.98%
CYP2D6 substrate - 0.8268 82.68%
CYP3A4 inhibition - 0.9454 94.54%
CYP2C9 inhibition - 0.7978 79.78%
CYP2C19 inhibition - 0.7374 73.74%
CYP2D6 inhibition - 0.8850 88.50%
CYP1A2 inhibition + 0.7107 71.07%
CYP2C8 inhibition - 0.9801 98.01%
CYP inhibitory promiscuity - 0.8341 83.41%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.5788 57.88%
Eye corrosion - 0.9336 93.36%
Eye irritation + 0.9757 97.57%
Skin irritation - 0.7199 71.99%
Skin corrosion - 0.8077 80.77%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8559 85.59%
Micronuclear + 0.5800 58.00%
Hepatotoxicity + 0.8375 83.75%
skin sensitisation - 0.8834 88.34%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.7429 74.29%
Nephrotoxicity + 0.5486 54.86%
Acute Oral Toxicity (c) III 0.4917 49.17%
Estrogen receptor binding - 0.8821 88.21%
Androgen receptor binding - 0.6518 65.18%
Thyroid receptor binding - 0.7505 75.05%
Glucocorticoid receptor binding - 0.7908 79.08%
Aromatase binding - 0.7218 72.18%
PPAR gamma - 0.6444 64.44%
Honey bee toxicity - 0.8801 88.01%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity - 0.9777 97.77%

Targets

Top

Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5697 Q9GZT9 Egl nine homolog 1 97.36% 93.40%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.31% 95.56%
CHEMBL2581 P07339 Cathepsin D 89.90% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.83% 86.33%
CHEMBL4208 P20618 Proteasome component C5 82.69% 90.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.50% 96.09%

Plants that contains it

Top
Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Ligularia cymbulifera

Cross-Links

Top
PubChem 45083666
LOTUS LTS0079357
wikiData Q105211350